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December 1, 1998Blood

The Life Cycle of Coagulation Factor VIII in View of Its Structure and Function

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Authors

PLPeter J. LentingInsermJMJan A. van MourikScripps Research InstituteKMKoen MertensUtrecht University

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Cite This Study

Lenting et al. (1998) studied this question.

synapsesocial.com/papers/6a1c4500a54fe8647d5ed976https://doi.org/10.1182/blood.v92.11.3983
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Mutations of factor VIII cleavage sites in hemophilia A1988 · 86 citations
  2. 2Liver endothelium mediates the hepatocyte's uptake of ceruloplasmin.1986 · 84 citations
  3. 3Purified human factor VIII procoagulant protein: comparative hemostatic response after infusions into hemophilic and von Willebrand disease dogs.1985 · 174 citations
  4. 4The Sequence Glu1811-Lys1818 of Human Blood Coagulation Factor VIII Comprises a Binding Site for Activated Factor IX1996 · 154 citations
  5. 5Low Prevalence of the Factor V Leiden Mutation Among “Severe” Hemophiliacs with a “Milder” Bleeding Diathesis1995 · 84 citations